A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706777



Internal ID130443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2479327..2479378hg38UCSC Ensembl
chr16:2529328..2529379hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432136
Supporting Variants
Samples
Known GenesTBC1D24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706777
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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